2-Chloro-5-5(trifluoromethyl)benzyl bromide

97%

  • Product Code: 116461
  Alias:    2-Chloro-5(trifluoromethyl)benzyl bromide
  CAS:    237761-77-2
Molecular Weight: 273.48 g./mol Molecular Formula: C₈H₅BrClF₃
EC Number: MDL Number: MFCD00236216
Melting Point: Boiling Point: 95°C/50mm
Density: 1.494 Storage Condition: room temperature
Product Description: This chemical is primarily used as an intermediate in the synthesis of various organic compounds, particularly in the pharmaceutical and agrochemical industries. Its structure, featuring a trifluoromethyl group and a benzyl bromide moiety, makes it a valuable building block for creating molecules with specific biological activities. It is often employed in the development of herbicides, fungicides, and other crop protection agents due to its ability to introduce fluorine atoms into target molecules, enhancing their efficacy and stability. Additionally, it plays a role in the production of active pharmaceutical ingredients (APIs) where the trifluoromethyl group can improve the metabolic stability and binding affinity of drugs. Its reactivity also makes it useful in cross-coupling reactions and other organic transformations in research and industrial settings.
Product Specification:
Test Specification
Purity (HPLC) 97-100
Refractive Index N20/D 1.5125
Appearance Yellow Liquid
Infrared Spectrum Conforms To Structure
Proton NMR Spectrum Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days £15.15
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5.000 10-20 days £53.15
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25.000 10-20 days £179.13
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2-Chloro-5-5(trifluoromethyl)benzyl bromide
This chemical is primarily used as an intermediate in the synthesis of various organic compounds, particularly in the pharmaceutical and agrochemical industries. Its structure, featuring a trifluoromethyl group and a benzyl bromide moiety, makes it a valuable building block for creating molecules with specific biological activities. It is often employed in the development of herbicides, fungicides, and other crop protection agents due to its ability to introduce fluorine atoms into target molecules, enhancing their efficacy and stability. Additionally, it plays a role in the production of active pharmaceutical ingredients (APIs) where the trifluoromethyl group can improve the metabolic stability and binding affinity of drugs. Its reactivity also makes it useful in cross-coupling reactions and other organic transformations in research and industrial settings.
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